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rs786203443

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786203443(C;T)
Make rs786203443(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position31358604
GeneNF1
is asnp
is mentioned by
dbSNPrs786203443
ebirs786203443
HLIrs786203443
Exacrs786203443
Varsomers786203443
Maprs786203443
PheGenIrs786203443
hapmaprs786203443
1000 genomesrs786203443
hgdprs786203443
ensemblrs786203443
gopubmedrs786203443
geneviewrs786203443
scholarrs786203443
googlers786203443
pharmgkbrs786203443
gwascentralrs786203443
openSNPrs786203443
23andMers786203443
23andMe allrs786203443
SNP Nexus

SNPshotrs786203443
SNPdbers786203443
MSV3drs786203443
GWAS Ctlgrs786203443
Max Magnitude0
ClinVar
Risk rs786203443(T;T)
Alt rs786203443(T;T)
Reference rs786203443(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NF1
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.29685622C>T
CLNSRC
CLNACC RCV000166752.1,